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Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Company Deals PIC

WestGene and CREATE Sign License Deal to Co‑Develop In Vivo CAR‑T Therapies

Fineline Cube Aug 31, 2026
Company Deals PIC

Simnova Closes nearly RMB 400 Million Series B to Advance CAR‑NK Candidate SNC103

Fineline Cube Aug 31, 2026
Company Deals PIC

Leaderna Therapeutics Closes Series A+ Led by Grand View Capital to Advance Oligonucleotide Pipeline

Fineline Cube Aug 31, 2026
Company Drug PIC

Eli Lilly Wins FDA Approval for Mounjaro Cardiovascular Risk Reduction in Type 2 Diabetes

Fineline Cube Aug 31, 2026
Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Fineline Cube Sep 1, 2026
Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Fineline Cube Sep 1, 2026
Company

Moderna Inc. Plans USD 1 Billion Investment in Shanghai for mRNA Vaccine Production

Fineline Cube Jul 6, 2023

US-based mRNA specialist Moderna Inc. (NASDAQ: MRNA) has revealed further details of its entry into...

Company Drug

CSPC Pharmaceutical Group Receives Marketing Approval for Desvenlafaxine in China

Fineline Cube Jul 6, 2023

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) has announced receiving marketing approval in China for...

Company Drug

AbbVie’s Rinvoq Receives NMPA Approval for Moderate to Severe Crohn’s Disease Treatment

Fineline Cube Jul 6, 2023

US pharmaceutical firm AbbVie (NYSE: ABBV) has announced receiving market approval from the National Medical...

Company Drug

Luye Pharma’s Goserelin Acetate Microspheres Approved by NMPA for Prostate Cancer Treatment

Fineline Cube Jul 5, 2023

Luye Pharma Group (HKG: 2186) has announced that it has received market approval from the...

Policy / Regulatory

CDE Releases 72nd Batch of Generic Reference Preparations with New Specifications

Fineline Cube Jul 5, 2023

The Center for Drug Evaluation (CDE) has released the 72nd batch of chemical generic reference...

Company Drug

Huadong Medicine’s Liraglutide Biosimilar Gains NMPA Approval for Weight Loss Indication

Fineline Cube Jul 5, 2023

China-based Huadong Medicine Co., Ltd (SHE: 000963) has announced that it has received additional indication...

Company Drug

Abbisko Therapeutics’ EGFR Inhibitor ABSK112 Clears FDA for Global Phase I NSCLC Study

Fineline Cube Jul 5, 2023

Shanghai-based biotech firm Abbisko Therapeutics Co., Ltd (HKG: 2256) has announced that it has received...

Company Drug

Jacobio Pharma’s KRAS Inhibitor Glecirasib Advances to Pivotal Pancreatic Cancer Trial

Fineline Cube Jul 5, 2023

China-based Jacobio Pharma (HKG: 1167) has announced that it has received the green light from...

Company Drug

InnoCare Pharma Initiates Clinical Trial for TYK2 Inhibitor ICP-488 in Psoriasis Patients

Fineline Cube Jul 5, 2023

China-based InnoCare Pharma (HKG: 9969, SHA: 688428) has announced a significant milestone in the clinical...

Company Medical Device

ZAP-X Gyroscopic Radiosurgery Platform Receives NMPA Approval for Brain Tumor Treatment

Fineline Cube Jul 5, 2023

US-based Zap Surgical Systems Inc. has announced that it has received market approval in China...

Company Drug

NMPA Approves Pitolisant for Narcolepsy-Related Excessive Daytime Drowsiness and Cataplexy

Fineline Cube Jul 5, 2023

The National Medical Products Administration (NMPA) has approved pitolisant as a treatment for excessive daytime...

Company Drug

Ascentage Pharma’s Olverembatinib Gets NMPA Greenlight for Phase III Study in Ph+ ALL

Fineline Cube Jul 5, 2023

China-based Ascentage Pharma (HKG: 6855) has announced that it has received approval from the National...

Company Drug

Amoytop Biotech’s Pegfilgrastim (Y Shape) Approved for Marketing by NMPA

Fineline Cube Jul 5, 2023

Xiamen-based Amoytop Biotech Co. Ltd (SHA: 688278) has received marketing approval from the National Medical...

Company Deals

Jacobio Pharma Retakes Global Rights to SHP2 Inhibitors After Terminating AbbVie Agreement

Fineline Cube Jul 5, 2023

China-based Jacobio Pharma (HKG: 1167) has announced the cancellation of a licensing agreement with US...

Company Medical Device

Helio Genomics’ Sister Company LAMH Wins NMPA Approval for Liver Cancer Test in China

Fineline Cube Jul 4, 2023

Helio Genomics has announced that its ‘sister company’ Laboratory for Advanced Medicine & Health Group...

Policy / Regulatory

NHSA Unveils Updated National Reimbursement Drug List Rules for 2023

Fineline Cube Jul 4, 2023

The National Healthcare Security Administration (NHSA) has released the updated rules that will govern this...

Company Deals

Binhui Biopharmaceutical and Topgene Biotechnology Partner for New Drug R&D and AI Platform Development

Fineline Cube Jul 4, 2023

Wuhan-based Binhui Biopharmaceutical and Hubei Topgene Biotechnology Co., Ltd have announced a strategic partnership to...

Company Drug

Huadong Medicine’s Mirvetuximab Soravtansine Heads for Priority Review by China’s CDE

Fineline Cube Jul 4, 2023

The China’s Center for Drug Evaluation (CDE) website has indicated that Huadong Medicine Co., Ltd...

Policy / Regulatory

NMPA Proposes Revisions to “Drug Inspection Management Measures”, Seeks Public Feedback

Fineline Cube Jul 4, 2023

The National Medical Products Administration (NMPA) has released revised provisions of the “Drug Inspection Management...

Company

Henlius Biotech Suspends IPO on STAR Market, Aims to Optimize Capital Strategy

Fineline Cube Jul 4, 2023

Shanghai Henlius Biotech Co., Ltd (HKG: 2696) has announced the suspension of its initial public...

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Recent updates

  • NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment
  • Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment
  • Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States
  • Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market
  • Laekna Doses First Patient in Phase I Study of LAE118 PI3Kα Inhibitor for Advanced Solid Tumors, Licensed to Vasque Bio for Up to USD 527 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Company Drug

Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States

Policy / Regulatory

Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market

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